activities either individually or as part of a team that may include the collection of field data, completing field tests, observation of construction activities, implementing health and safety procedures, oversight of related subcontractor services and other field related activities; Field duties may include drilling oversight, well installation, analytical sampling, gauging and surveying activities, operation and maintenance of remediation systems; Assisting in the field sampling and testing of various environmental media; Compiling and completing field data for multiple sites; Client interaction and communication; Candidate must have ability to work independently with minimal supervision;
Coordination with task and project managers, working with on-site subcontractors and field staff; Calibrating and maintaining field instrumentation, QA/QC data sheets and field logs in support of environmental investigations; Performing field activities related to environmental compliance, stormwater pollution prevention and erosion and sediment control inspections and reporting; Assisting with the development and distribution of field notes, meeting minutes, project action item lists, internal tracking of projects activities and general project coordination activities in support of project managers; Assisting in the field interpretation of project design drawings and technical specifications
and communicating findings with the project engineers and geologists; Position Requirements and Qualifications: Bachelor's Degree in Geology, Environmental Science or other science related field.
Will also consider commensurate combination of education and experience. Must be able to work in both indoor and outdoor environments Valid Driver's License and ability to authorize our review of a motor vehicle driving record for the past 5 years; Ability to work using hand tools and testing equipment; Required to lift objects of up to 50 lbs Consistent travel for field work required locally and throughout the Southeastern United States Good written and verbal communication skills; Basic knowledge in the operation of smart phones and computers for communication and recording time worked Must pass a pre-employment background and drug test Job Posted by Applicant Pro
new services, we never forget the values that made us who we are as a company. We are a team. A family. A group of smart, talented, big-hearted individuals working together for the success of our customers and the growth of our communities. AND WE HONOR OUR COMMITMENTS What we do at Ortec is complicated at times.
Why we do what we do is not complicated: We want to make a difference for our customers and our communities around us. How we do what we do is also not complicated: everything starts with Integrity. WHY ORTEC? The foundation of Ortec is our talented, dedicated employees. Our commitment to delivering chemical manufacturing services with measurable quality has made us a trusted
partner to some of the most familiar names in business. Our success is drawn from the experience, energy and teamwork of our employees, who consistently deliver results by anticipating change and executing solutions with confidence and passion.
At Ortec, you'll be working with the latest technologies and tools, not to mention some of the industry's best and brightest minds. From the top down, this type of commitment and energy is radiated throughout the company. The result is a growing, dynamic, and rewarding place to work a company where we work as many and we win as one. You are a name, not a number! We offer an excellent benefit package, including: Competitive benefits with onsite
medical care for free401k with match Medical, Dental, and Vision and much more!
POSITION SUMMARY Serve as a focal point for providing technical support and expertise to manufacturing and plant operations. Provide hands-on support to production, sales, lab, and customers on technical issues for current and future technology. ESSENTIAL FUNCTIONS Provide in-depth, thorough knowledge of Production processes, equipment, and operations. Communicate and interact with customers or potential customers, regarding processes, technology, production logistics, quality, and safety. Investigate the root cause of customer complaints and recommend corrective actions. Observe, critique and optimize chemical processes in safety, efficiency, quality, performance, technical aspects.
Lead in the scale up of new products from lab to plant trials. Develop, improve, and customize products, equipment, formulas, processes, and analytical methods in support of customers. Participate and lead in technical meetings relating to manufacturing operations, product quality, and production efficiency. Coordinate technology transfer to and from customers. Provide work direction, technical training, and guidance to operations. Direct, coordinate, and advise personnel in test procedures for analyzing components and physical properties of materials relating to new technology or customer methods.
Monitor process and quality data for trends and cause/effect analysis.
will assist to ensure methods are accurate, precise, and robust for use of testing release samples. The QCCII must have a strong understanding of experimental design, chemical theory and analytical instrumentation such as HPLC, GC, ICP-MS/ICP-OES. The QCCII must be knowledgeable in all QC routine functions and capable of being relied upon to perform any and all QC related functions.
The QCCII is expected to be capable of independently executing in-house methods and procedures and performing them as written with little to no assistance based on their extensive experience. Perform release, stability and special request testing of finished products and raw materials following Standard Operating
Procedures (SOPs), in-house test methods, and/or compendial methods. Be able to make decisions based on facts, experience and intelligent backssment. Independently manage projects assigned by management within expected/established time frames.
Stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the QC Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices. Assist laboratory personnel in resolving Out of Specification (OOS) results in accordance with laboratory investigation procedures if assigned. Assist in training of new laboratory personnel and document training in accordance
with established laboratory SOPs and the Nutramax training program.
Follow current Good Manufacturing Practice (c GMP) documentation guidelines to record all procedures in a timely fashion. Maintain a safe work environment and will ensure that all equipment used in the testing procedures is calibrated and properly maintained. Perform other assigned duties as may be required in meeting company objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements: Five or more years of laboratory experience in a c GMP facility, including experience with operation of laboratory instrumentation including Gas Chromatography (GC) and/or Liquid Chromatography (LC) required, troubleshooting, project management, generation and revision of SOPs and test methods.
Method optimization, validation and/or development experience is a requirement for this position. Effective interpersonal, self-motivation, communication skills and the ability to interact with all levels of personnel are required. Education and Experience: A Bachelor of Science (B. S. ) or Bachelor of Arts (B. A. ) degree in a science-related field such as Chemistry, Biochemistry or Biology preferred. Supervisory Responsibilities: N one Job Posted by Applicant Pro
· Support staff member, serving as a laboratory technician under the Toxicology / Physiology Program. · Conduct oyster shell deposition toxicity assays for PFAS-free AFFF chemicals. · Assist with laboratory and mesocosm toxicology assays and with field collections as requested.
· Assist in data analysis, report and manuscript writing. · Support NCCOS scientists in sample tracking and logging, data entry into electronic databases, and general laboratory support, such as glassware preparation Experience Requirements: · Master's degree in Biology or related discipline with experience working in a laboratory setting. · Knowledge/experience in oyster physiology. · Ability to conduct independent
research, analyze data, and prepare reports. · Experience with aquatic animal physiology and toxicity testing, particularly bivalve. · Experience with dissection, tissue homogenization, microscopy, physiological analyses.
· Ability to support student researchers. · Ability to compile standard operating procedures (SOP), implement and follow good laboratory practices (GLP). · Good written and oral communication skills. CSS is predominantly a Federal Contractor and is subject to following the terms of Executive Orders. CSS requires all Employees (Direct, Indirect, government, state, and commercial), including employees working from home/remotely, to be fully vaccinated against COVID-19
or have an approved exemption. Exceptions to the COVID-19 vaccine requirements may be provided to individuals for religious beliefs or medical reasons.
Requests for an exception must be submitted to the CSS HR Department. CSS is an Equal Opportunity/Affirmative Action Employer who provides equal employment opportunities to all employees and applicants for employment without regards to race, color, religion, interaction, gender identity, interactionual orientation, pregnancy, national origin, age, disability, veteran status or genetic information. In addition to federal law requirements, CSS complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
is integral to advancing NCCOS' Stressor Detection & Impacts strategic science objectives via developing and deploying innovative coastal observing technologies to support early detection, predictive modeling, ecological forecasting, and backssment of impacts on coastal resources and economies.
Currently the research focuses on detection and monitoring of harmful algal blooms and their toxins in marine and freshwater (Great Lakes) systems. The successful applicant will have a demonstrated familiarity and ability to work with biosensing technologies (e. g. antibody-based techniques, surface plasmon resonance (SPR), waveguides, electrochemical sensors). Duties include: • Assists researchers
in developing antibody-based assays for autonomous and field-portable biosensors to detect harmful algae and their toxins; • Implements established SOPs and QA/QC procedures for printing protein arrays and executing SPR surface chemistry protocols, and assists researchers in method development; • Assists in maintaining biosensor/ bioanalytical instrumentation (e.
g. SPR instrument); • Maintains up-to-date, well-organized, and highly detailed laboratory notebook covering all relevant research activities/experiments; • Collects, performs preliminary analyses of, and reports on experimental data to research personnel and supervising scientist; • Responsible for general laboratory maintenance
including, but not limited to, washing/ autoclaving glassware, preparing algal culture media, maintaining laboratory equipment, inventory of supplies/reagents, etc.
Qualifications: • Bachelor of Science degree in biological sciences, biochemistry, or related discipline (including at least 2 years of chemistry coursework), or some combination of education and two years of progressively responsible, relevant work experience equivalent; • Demonstrated ability to conduct and assist in the development of complex research protocols for biosensor/ bioanalytical instrumentation while maintaining safe laboratory practices; • Demonstrated ability to learn to operate, maintain, and troubleshoot sensitive biosensor/ bioanalytical instrumentation and novel technologies; • Demonstrated ability/ skills in analysis, organization, and communication of scientific data; • Ability to work individually and as part of a team, with strong interpersonal as well as written and oral communication skills; • Ability to calculate molarity, sample dilutions, standard curve concentrations, and execute other basic chemical formulas essential; • Basic mechanical knowledge and a strong level of manual dexterity required; ability to conduct minor repairs and modifications to electromechanical fluidic sensor devices as directed; • Experience with sterile technique preferred; • Highly proficient in MS Office applications, familiarity with statistical software and Matlab beneficial, and ability to learn/apply new application-specific software packages as required.
Physical requirements: • Ability to work proficiently with computer keyboards and screens; • Ability to move about a chemistry lab and complete bench-level tasks safely and efficiently; • Ability to lift 35 lbs. CSS is predominantly a Federal Contractor and is subject to following the terms of Executive Orders.
CSS requires all Employees (Direct, Indirect, government, state, and commercial), including employees working from home/remotely, to be fully vaccinated against COVID-19 or have an approved exemption. Exceptions to the COVID-19 vaccine requirements may be provided to individuals for religious beliefs or medical reasons. Requests for an exception must be submitted to the CSS HR Department. CSS is an Equal Opportunity/Affirmative Action Employer who provides equal employment opportunities to all employees and applicants for employment without regards to race, color, religion, interaction, gender identity, interactionual orientation, pregnancy, national origin, age, disability, veteran status or genetic information.
In addition to federal law requirements, CSS complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Unparalleled schedule flexibility and supportive company culture Dynamic company partnerships to ensure career stability Meaningful work-life balance with flexible schedules Highly competitive rates + 401K Plan with company match Healthcare benefits package Online CEU Credits Promotion / Advancement / Transfer Opportunities Referral bonus program eligibility Employee Assistance Program Excellent management and support team Student mentor program We offer additional benefits and perks, please reach out today About Us: Tender Touch Rehab is part of Enhance Therapies , a family of therapy companies with more than 30 years of industry leading experience.
With over 7,000 therapists in 28 states
and growing, we provide quality rehabilitation services to homecare, sub-acute, long-term care, outpatient, hospital, and assisted living facilities throughout the nation.
Why become a Physical Therapist with Tender Touch Rehab? Company Culture - Become part of a close-knit team of passionate clinicians who strive to professionally develop and grow together through collaboration. Compensation Package - Competitive rates, full benefits package, 401k plan, continuing education allowance and much more. Clinical Advancement - Additional training, mentorship, and direct support to help develop your career. Opportunities - Focus on the setting YOU are passionate about! Upward Mobility/Leadership
Oversight - A focus on promoting success through therapists invested in leadership roles and internal promotions.
Quality Care Starts with US - We demonstrate empathy and compassion to all team members and patients whom we treat. Ways to Get Involved - Clinical mentorship and community outreach opportunities. Qualifications: Physical Therapist provides a comprehensive physical therapy evaluation based on MD’s orders. Physical Therapist provides comprehensive treatment plans including long and short-term goals, frequency, duration, and treatment modalities. PT ensures MD orders are obtained for evaluations, treatments, re-certifications, and discharges.
PT Provides comprehensive treatment to patients utilizing modalities and modify patient treatment as indicated while adhering to precautions. Physical Therapist completes all required documentation Requirements: Graduate of an accredited university with a B. S. Doctorate, MA, or MS in Physical Therapy that the APTA recognizes PT holds a current license and/or registration as a Physical Therapist in-state (as applicable)#TT1 Pay Range: USD $39.00 - USD $55.00 /Hr. For more details: jobs-search. org/physical-therapist_sumter-c446314/job_i1965995493
and reports lab results; performs operational duties, maintenance and advanced troubleshooting of laboratory instrumentation and equipment. Tenet South Carolina Job ID #230504xyz X. For more details: jobs-search. org/sciences_rock-hill-c446399/job_i1956682018
work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, medical and cosmetic product testing and in agroscience Contract Research Organisation services.
It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular
clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries.
Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description We are seeking a mass spectrometry lead scientist who will be responsible for leading
the development and optimization of our mass spectrometry-based workflows in Analytical Development/Validation for small molecules, peptides, and oligonucleotides Employee Responsibilities: Function as an MS subject matter expert within Analytical Development and be viewed as peer to other MS SMEs within Eurofins network Perform method development, feasibility, qualification and/or validation of methods in support of biomedical products using primarily Mass spectrometry Execute identification of unknown compounds with minimal support Develop and execute validation plans Troubleshoot method and instrumentation problems Generate complete, accurate, and concise documentation using electronic systems and laboratory notebook Author documents (e.
g. development reports, methods and client reports) Give presentations for training and client reviews Have a strong understanding of current regulatory expectation Effectively guide more junior scientists on technical issues Use office and instrumentation specific computer software Qualifications B. S. / M. S. degree in Chemistry, Biology, biochemistry or related technical discipline with 4+ years of relevant experience, either post-doctoral or in the bio/medical industry Hands-on experience in use of multiple types of mass spectrometers (GC/MS, LC/MS, HRMS) Experience with identification of unknown materials Ability to work independently and as part of a team with internal and external clients, self-motivation, adaptability, and a positive attitude.
Strong organizational and time management skills Excellent communication (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Authorization to work in the United States indefinitely without restriction or sponsorship.
Additional Information Position is full-time position, Monday - Friday 8:00pm - 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Hardeeville, S. C. serving the medical and healthcare needs of Jasper and Beaufort counties since November 2004. Hilton Head Hospital (HHH) is a 109-bed acute care hospital located on Hilton Head Island, S. C. Opened in 1974, HHH serves Hilton Head Island, Bluffton, Okatie and surrounding counties.
All facilities are owned and operated by Dallas-based Tenet Healthcare Corp. Both hospitals are accredited by The Joint Commission, the nation’s oldest and largest hospital accreditation agency. Learn more about Hilton Head Regional Healthcare at About Hilton Head Hospital Hilton Head Hospital (HHH) is a 109-bed acute care hospital located at 25 Hospital Center Boulevard in Hilton Head Island,
SC. Opened in 1974, HHH serves Hilton Head Island, Bluffton, Okatie and surrounding counties through its care team of over 600 colleagues and over 100 physicians.
The hospital provides a continuum of services through its centers and programs, including a 24-hour emergency department, critical care, cardiac care ranging from minimally invasive to open heart surgery, obstetrics/gynecology, urology, a nationally accredited breast health center, spine care, gastroenterology, surgical services, cardiac and physical rehabilitation, and a 12-bed geriatric psychiatric inpatient unit. To learn more about Hilton Head Hospital, please visit RN Case Manager Full Time Days Position Summary The RN
Case Manager is responsible to facilitate care along a continuum through effective resource coordination to help patients achieve optimal health, access to care and appropriate utilization of resources, balanced with the patient’s resources and right to self-determination.
The individual in this position has overall responsibility for ensuring that care is provided at the appropriate level of care based on medical necessity and to backss the patient for transition needs to promote timely throughput, safe discharge and prevent avoidable readmissions. This position integrates national standards for case management scope of services including: Utilization Management supporting medical necessity and denial prevention Transition Management promoting appropriate length of stay, readmission prevention and patient satisfaction Care Coordination by demonstrating throughput efficiency while assuring care is the right sequence and at appropriate level of care Compliance with state and federal regulatory requirements, TJC accreditation standards and Tenet policy Education provided to physicians, patients, families and caregivers Leads a population of patients by service line.
Responsibilities Precepts new staff members and acts as resource to all staff. Facilitates TEMPO as needed.
Participates in department Quality improvement initiatives. At least one committee participation or major Projects as assigned RN CASE MANAGER FULL TIME DAYS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE. Education Required: Graduate of an accredited school of nursing. Academic degree in nursing (bachelor's or master's). Preferred: Academic degree in nursing (bachelor's or master's). Experience Required: 2 years of acute hospital patient care experience. Preferred: Acute hospital case management experience. Certifications Required: RN.
Must be currently licensed, certified or registered to practice profession as required by law or regulation in state or practice or policy. Active RN license for state(s) covered. Preferred: Accredited Case Manager (ACM) Physical Demands Lift/position up to 25 lbs. Push/pull up to 25 lbs. of force. Frequent sitting. Moderate standing, walking, reaching, stooping, or bending. Manual dexterity, mobility, touch, auditory to perform all the related duties of the position. 230505xyz XEmployment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, interaction (including pregnancy), national origin, age, disability, genetic information, interactionual orientation, gender identity or expression, veteran status or any other legally protected status.
Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. For more details: jobs-search. org/sciences_hilton-head-island-c446394/market-rn-case-manager-ft-days-hilton-head-island_i1961775218
Analytical Chemistry (AC) Management. Performs Quality Control testing and data review to support timely release of product in weekly basis. Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies.
Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry. backss testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and
testing parameters were properly followed. Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group.
Mentor and train chemists in the proper execution, including interpretation of validation studies. Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage. Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives. Communicate effectively with other
departments within the organization and function within a team environment.
Regular attendance is required. Minimum Requirements: Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses. Must be proficient on laboratory instrument trouble shooting. In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products. Knowledge i n most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods. Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry.
Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner. Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation. Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data.
Detailed knowledge of principles of routine laboratory operations. Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to medical and/or nutritional supplement GLP/GMP is strongly desired. Demonstrated aptitude to function in a dynamic fast-paced environment. Education and Experience A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or medical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred.
Extensive experience may be accepted in lieu of an advanced degree. A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred. A need to work on the bench to accomplish tasks along with the Analytical Chemistry team. Supervisory Responsibilities: None Job Posted by Applicant Pro
our first MIGS device-the i Stent®-in the United States, followed by our next-generation i Stent inject® device in September 2018. In November 2019, Glaukos acquired Avedro, maker of the first and only FDA-approved cross-linking technology for progressive keratoconus.
And we continue to seek to leverage our platform technologies to build a comprehensive and proprietary portfolio of micro-scale surgical and medical therapies for glaucoma, corneal health, and retinal diseases. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol " GKOS" Our global headquarters is located in Aliso Viejo,
California with additional locations in San Clemente, California and Burlington, Massachusetts. How will you make an impact? The Senior RBM is responsible for training and helping to integrate the i Stent technology into their assigned practice.
You will achieve quarterly sales objectives by selling to targeted ophthalmic surgeons within the assigned territory. The Senior RBM will attend surgeries and help the surgeon to achieve the desired surgical outcomes for the patient. The Senior RBM will achieve these standards by focusing on the customer while managing the territory for the best return on investment. What will you do? Prospecting by initiating sales calls to sell the surgeon
on the Glaukos i Stent and initiate surgical wet-labs to train the surgeon.
Attend the initial i Stent surgeries until the surgeon is confident and skilled to perform the cases. Attend surgeries as needed to update on new techniques to improve surgical outcomes. Train the office staff and the doctor to recognize and convert patients to the i Stent technology using Glaukos Practice System (GPS). Work with the surgeon and staff to educate and assist in getting proper reimbursement for the Glaukos i Stent. Attend targeted meetings as directed to increase sales lead opportunities and protect existing business. How will you get here? Education: Bachelor's degree required.
Concentration in Business or Marketing preferred. Requirements: 3 plus years of ophthalmic medical sales experience (either surgical or medical). The preferred candidate would have both ophthalmic surgical and medical experience. Experience developing and expanding new territories. Proven experience meeting and exceeding targeted goals. Ability to build relationships and interact with all levels. Ability to communicate with KOLs and surgeons both in the OR and outside. Proven ability to build and retain customer base. Experience with tracking CRM software. Ability to work within a budget.
Ability to comply with procedures and processes. Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family. Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we're a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others.
We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last two years!
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction including interactionual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. ABOUT US Founded in 1998, Glaukos Corporation is an ophthalmic medical technology and medical company focused on novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our company was the first company to bring to market Micro-Invasive Glaucoma Surgery (MIGS), the micro-invasive procedure which revolutionized the treatment and management of glaucoma. In 2012, we launched our first MIGS device-the i Stent®-in the United States, followed by our next-generation i Stent inject® device in September 2018 and i Stent inject® W in September 2020. In November 2019, Glaukos acquired Avedro, maker of the first and only FDA-approved cross-linking technology for progressive keratoconus. And we continue to seek to leverage our platform technologies to build a comprehensive and proprietary portfolio of micro-scale surgical and medical therapies for glaucoma, corneal health, and retinal diseases.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol " GKOS" Our global headquarters is located in San Clemente, California with additional locations in Waltham and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employmentwithout regard to race, color, religion, interaction including interactionual orientation and genderidentity, national origin, disability, protected Veteran Status, or any othercharacteristic protected by applicable federal, state, or local law.
Science Jobs refers to a category of employment that specializes in the field of science, encompassing a diverse range of professions including researchers, laboratory technicians, science educators, and many others engaged in scientific disciplines. These jobs are characterized by their focus on inquiry, exploration, and the application of scientific methods to understand the natural world. They often require a strong educational background in science, critical thinking, problem-solving skills, and sometimes, experience with specialized equipment or software. In today's world, Science Jobs are crucial for innovation, technological advancement, and addressing complex challenges in healthcare, environment, and industry.
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Science Jobs are specialized career paths within the field of science that encompass a wide range of disciplines such as biology, chemistry, physics, environmental science, and more. These jobs often require a strong educational foundation and specialized training. Key features of science jobs include a focus on research and development, data analysis, and the practical application of scientific knowledge to solve real-world problems. Additionally, professionals in science jobs are typically engaged in expanding the frontiers of scientific understanding and contributing to technological and medical advancements. These roles can be found in academia, government agencies, private sector research labs, and industrial settings.
Science Jobs are career positions specifically within the wide domain of science, spanning across various disciplines including biology, chemistry, physics, and environmental science, among others. These jobs often feature a focus on research, development, innovation, and exploration. They can be found within academic institutions, private sector companies, research organizations, and government agencies. Characteristics of science jobs include a strong emphasis on analytical skills, problem-solving, critical thinking, and a commitment to continuous learning to keep pace with evolving scientific knowledge and technological advancements.
